chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5432156	5432157	G	T	13	GENIC	homozygous	119766598
20	5432230	5432231	C	A	8	GENIC	homozygous	119766600
20	5432274	5432275	C	T	7	GENIC	heterozygous	119766601
20	5432354	5432355	C	A	19	GENIC	homozygous	119766607
20	5432525	5432526	A	G	12	GENIC	homozygous	109077938
20	5432683	5432684	T	C	11	GENIC	homozygous	109077940
20	5432981	5432982	A	G	21	GENIC	homozygous	109077942
20	5433695	5433696	T	C	7	GENIC	homozygous	109077944
20	5433909	5433910	G	A	23	GENIC	homozygous	109077946
20	5434025	5434026	G	A	13	GENIC	homozygous	109077948
20	5435531	5435532	T	C	10	GENIC	homozygous	109077952
20	5435668	5435669	G	A	20	GENIC	homozygous	109296935
20	5436238	5436239	G	T	24	GENIC	homozygous	109296937
20	5436340	5436341	T	C	23	GENIC	homozygous	109455594
20	5436355	5436356	T	C	13	GENIC	homozygous	119766624
20	5436376	5436377	G	C	9	GENIC	heterozygous	109455596
20	5436478	5436479	G	T	22	GENIC	homozygous	109077954
20	5436873	5436874	C	G	13	GENIC	homozygous	109077956
20	5436902	5436903	C	A	4	GENIC	homozygous	109077958
20	5436916	5436917	G	A	5	GENIC	homozygous	109077964
20	5437389	5437390	T	C	12	GENIC	homozygous	109296939
20	5437715	5437716	A	G	18	GENIC	homozygous	109077970
20	5438747	5438748	G	A	11	GENIC	homozygous	109077974
20	5438756	5438757	T	C	11	GENIC	homozygous	109077976
20	5438758	5438759	G	T	11	GENIC	homozygous	109077978
20	5438793	5438794	G	A	21	GENIC	homozygous	109077980
20	5438830	5438831	G	T	27	GENIC	homozygous	109077982
20	5440335	5440336	T	G	25	GENIC	homozygous	109077984